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PUBMED FOR HANDHELDS

Journal Abstract Search

342 related items for PubMed ID: 1483593

  • 41.
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  • 42. Megakaryocytes from the marrow of a patient with Glanzmann's thrombasthenia lacked GP IIb-IIIa complexes.
    Hourdillé P, Fialon P, Belloc F, Namur M, Boisseau MR, Nurden AT.
    Thromb Haemost; 1986 Aug 20; 56(1):66-70. PubMed ID: 3535160
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  • 43. Platelet adhesion to fibrin(ogen).
    Endenburg SC, Hantgan RR, Sixma JJ, de Groot PG, Zwaginga JJ.
    Blood Coagul Fibrinolysis; 1993 Feb 20; 4(1):139-42. PubMed ID: 8457642
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  • 48. Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families.
    Sandrock K, Halimeh S, Wiegering V, Kappert G, Sauer K, Deeg N, Busse E, Zieger B.
    Klin Padiatr; 2012 Apr 20; 224(3):174-8. PubMed ID: 22513797
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  • 49.
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  • 50. Normal synthesis and expression of endothelial IIb/IIIa in Glanzmann's thrombasthenia.
    Giltay JC, Leeksma OC, Breederveld C, van Mourik JA.
    Blood; 1987 Mar 20; 69(3):809-12. PubMed ID: 3545321
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  • 51. A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIa.
    Losonczy G, Rosenberg N, Kiss C, Kappelmayer J, Vereb G, Kerényi A, Balogh I, Muszbek L.
    Thromb Haemost; 2005 May 20; 93(5):904-9. PubMed ID: 15886807
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  • 52. Role of RFLP using TspRI for carrier detection in Glanzmann's thrombasthenia: a report on two families.
    Kannan M, Yadav BK, Ahmad F, Saxena R.
    Int J Lab Hematol; 2010 Feb 20; 32(1 Pt 1):e158-62. PubMed ID: 19170775
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  • 53.
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  • 54. Truncation of glycoprotein (GP) IIIa (616-762) prevents complex formation with GPIIb: novel mutation in exon 11 of GPIIIa associated with thrombasthenia.
    Ferrer M, Tao J, Iruín G, Sánchez-Ayuso M, González-Rodríguez J, Parrilla R, González-Manchón C.
    Blood; 1998 Dec 15; 92(12):4712-20. PubMed ID: 9845537
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  • 55. An exon 28 mutation resulting in alternative splicing of the glycoprotein IIb transcript and Glanzmann's thrombasthenia.
    Iwamoto S, Nishiumi E, Kajii E, Ikemoto S.
    Blood; 1994 Feb 15; 83(4):1017-23. PubMed ID: 8111043
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  • 56.
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  • 57. Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia.
    Tokgoz H, Torun Ozkan D, Caliskan U, Akar N.
    Platelets; 2015 Feb 15; 26(8):779-82. PubMed ID: 25734216
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  • 58. A point mutation in the cysteine-rich domain of glycoprotein (GP) IIIa results in the expression of a GPIIb-IIIa (alphaIIbbeta3) integrin receptor locked in a high-affinity state and a Glanzmann thrombasthenia-like phenotype.
    Ruiz C, Liu CY, Sun QH, Sigaud-Fiks M, Fressinaud E, Muller JY, Nurden P, Nurden AT, Newman PJ, Valentin N.
    Blood; 2001 Oct 15; 98(8):2432-41. PubMed ID: 11588040
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  • 59. A novel (288delC) mutation in exon 2 of GPIIb associated with type I Glanzmann's thrombasthenia.
    Tao J, Arias-Salgado EG, González-Manchón C, Díaz-Cremades J, Ayuso MS, Parrilla R.
    Br J Haematol; 2000 Oct 15; 111(1):96-103. PubMed ID: 11091187
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  • 60.
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